Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP820258.RAEuXqVBO19oaI_0h5EoTPH9cOkk3cSClvWOOZVdbx8_A130_assertion> ?p ?o ?g. }
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- NP820258.RAEuXqVBO19oaI_0h5EoTPH9cOkk3cSClvWOOZVdbx8_A130_assertion type Assertion NP820258.RAEuXqVBO19oaI_0h5EoTPH9cOkk3cSClvWOOZVdbx8_A130_head.
- NP820258.RAEuXqVBO19oaI_0h5EoTPH9cOkk3cSClvWOOZVdbx8_A130_assertion description "[The frequency of heterozygotes for the 20210A prothrombin allele was 6.5% among patients and 2.8% among controls (OR 2.4, 95% CI 1.0-5.9), increasing to 8.7% in patients with a family history of myocardial infarction (OR 3.3, 95% CI 1.2-9.1), to 9.9% in patients (n=81) with < or =1 vessel disease (OR 3.8, 95% CI 1.3-10.8), and to 13.0% in patients who were normocholesterolaemic, non-diabetic, normotensive and non-smokers (OR 5.1, 95% CI 1.2-21.4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP820258.RAEuXqVBO19oaI_0h5EoTPH9cOkk3cSClvWOOZVdbx8_A130_provenance.
- NP820258.RAEuXqVBO19oaI_0h5EoTPH9cOkk3cSClvWOOZVdbx8_A130_assertion evidence source_evidence_literature NP820258.RAEuXqVBO19oaI_0h5EoTPH9cOkk3cSClvWOOZVdbx8_A130_provenance.
- NP820258.RAEuXqVBO19oaI_0h5EoTPH9cOkk3cSClvWOOZVdbx8_A130_assertion SIO_000772 11741359 NP820258.RAEuXqVBO19oaI_0h5EoTPH9cOkk3cSClvWOOZVdbx8_A130_provenance.
- NP820258.RAEuXqVBO19oaI_0h5EoTPH9cOkk3cSClvWOOZVdbx8_A130_assertion wasDerivedFrom befree-20140225 NP820258.RAEuXqVBO19oaI_0h5EoTPH9cOkk3cSClvWOOZVdbx8_A130_provenance.
- NP820258.RAEuXqVBO19oaI_0h5EoTPH9cOkk3cSClvWOOZVdbx8_A130_assertion wasGeneratedBy ECO_0000203 NP820258.RAEuXqVBO19oaI_0h5EoTPH9cOkk3cSClvWOOZVdbx8_A130_provenance.